Le Winter M M, Curtis G P, Engler R L, Shabetai R, Verba J
Clin Pharmacol Ther. 1979 Aug;26(2):162-6. doi: 10.1002/cpt1979262162.
Nadolol, a recently developed noncardioselective beta-adrenergic blocker, has the potential advantages of a longer oral half-life (t 1/2) than propranolol and, in animal studies, markedly fewer direct myocardial depressant effects. Neither the relative intravenous potency of nadolol and propranolol nor the comparative effects of the 2 drugs on left ventricular performance has been studied in man. We compared equiblocking intravenous doses of nadolol and propranolol in 10 subjects with ischemic wall-motion disorders. Nadolol was on the average 6.2 times as potent on a milligram-for-milligram basis. Both drugs decreased resting heart rate (p less than 0.02) and produced small rises in both mean pulmonary artery (p less than 0.03) and mean pulmonary artery wedge (p less than 0.03) pressures without significantly reducing the cardiac output. Both drugs also produced depression of the radionuclide ejection fraction (p less than 0.002). There were no significant differences between the effects of the 2 drugs on any of the aforementioned variables. Thus, the effects of nadolol on left ventricular performances are similar to those of propranolol. Because of its long oral t 1/2, nadolol may prove to be a clinically useful drug.
纳多洛尔是一种最近研制出的非选择性β肾上腺素能阻滞剂,它比普萘洛尔具有口服半衰期(t1/2)更长的潜在优势,并且在动物研究中,其直接心肌抑制作用明显较少。纳多洛尔和普萘洛尔的相对静脉效价以及这两种药物对左心室功能的比较作用在人体中尚未进行研究。我们在10名患有缺血性室壁运动障碍的受试者中比较了等剂量静脉注射纳多洛尔和普萘洛尔的效果。纳多洛尔按毫克计算平均效力是普萘洛尔的6.2倍。两种药物均降低静息心率(p<0.02),并使平均肺动脉压(p<0.03)和平均肺动脉楔压(p<0.03)略有升高,而心输出量无显著降低。两种药物还使放射性核素射血分数降低(p<0.002)。两种药物对上述任何变量的作用均无显著差异。因此,纳多洛尔对左心室功能的影响与普萘洛尔相似。由于其口服t1/2长,纳多洛尔可能被证明是一种临床上有用的药物。